Thiazol-5-ylmethyl ((2R,5R)-5-amino-1,6-diphenylhexan-2-yl)carbamate hydrochloride

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Reagent Code: #229316
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CAS Number 1247119-33-0

science Other reagents with same CAS 1247119-33-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 446.01 g/mol
Formula C₂₃H₂₈ClN₃O₂S
badge Registry Numbers
MDL Number MFCD28100862
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of protease inhibitors, particularly for the development of antiviral agents. Shows potential in the design of enzyme inhibitors targeting specific metabolic pathways in disease states. Its structure supports high selectivity and binding affinity, making it valuable in optimizing drug candidates for improved efficacy and stability. Also employed in structure-activity relationship (SAR) studies to enhance pharmacokinetic properties of therapeutic molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿17,510.00
Thiazol-5-ylmethyl ((2R,5R)-5-amino-1,6-diphenylhexan-2-yl)carbamate hydrochloride
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Used in pharmaceutical research as a key intermediate in the synthesis of protease inhibitors, particularly for the development of antiviral agents. Shows potential in the design of enzyme inhibitors targeting specific metabolic pathways in disease states. Its structure supports high selectivity and binding affinity, making it valuable in optimizing drug candidates for improved efficacy and stability. Also employed in structure-activity relationship (SAR) studies to enhance pharmacokinetic properties of

Used in pharmaceutical research as a key intermediate in the synthesis of protease inhibitors, particularly for the development of antiviral agents. Shows potential in the design of enzyme inhibitors targeting specific metabolic pathways in disease states. Its structure supports high selectivity and binding affinity, making it valuable in optimizing drug candidates for improved efficacy and stability. Also employed in structure-activity relationship (SAR) studies to enhance pharmacokinetic properties of therapeutic molecules.

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